scispace - formally typeset
S

Satoru Motoyama

Researcher at Kobe University

Publications -  17
Citations -  465

Satoru Motoyama is an academic researcher from Kobe University. The author has contributed to research in topics: Genotype & Population. The author has an hindex of 10, co-authored 17 publications receiving 432 citations. Previous affiliations of Satoru Motoyama include University of Oxford.

Papers
More filters
Journal Article

The role of human papilloma virus in the molecular biology of cervical carcinogenesis.

TL;DR: A large body of knowledge already generated in this area supports the view that high-risk HPV types have the ability to transform cells into a malignant phenotype, but it remains unclear how and when cofactors or factors that are innate in the HPV-infected cells launch the host cells into an irreversible progression to carcinoma.
Journal Article

Mutational analysis of BRCA1 and BRCA2 and clinicopathologic analysis of ovarian cancer in 82 ovarian cancer families: two common founder mutations of BRCA1 in Japanese population.

TL;DR: The results indicate that the features of BRCA-associated ovarian cancer in Japan appear to be similar to those in Western countries, and the L63X and Q934X mutations of B RCA1 seem to be common founder mutations unique to the Japanese population.
Journal ArticleDOI

Clinical outcomes of uterine sarcomas: results from 14 years worth of experience in the Kinki district in Japan (1990-2003).

TL;DR: Analysis of clinical outcomes and therapeutic varieties in Japan from 1990 to 2003 showed that aggressive surgery including EH or RH at the time of initial operation offers the possibility of prolonged survival, and younger age, early stage, and surgical procedure were associated with significantly better OAS.
Journal ArticleDOI

Vaginoplasty with Interceed absorbable adhesion barrier for complete squamous epithelialization in vaginal agenesis.

TL;DR: This innovative surgical procedure may be a potential alternative approach for the therapy of vaginal agenesis with the use of the absorbable adhesion barrier Interceed with excellent results.
Journal ArticleDOI

Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25.

TL;DR: To explore whether the candidate gene in this 3p22-p25 region contributed to carcinogenesis of familial ovarian cancer in a similar fashion to the tumor suppressor gene, it was observed that the frequency of LOH at four markers in this region was >50% only in tumor tissues from patients with no mutation in BRCA1 or BRC a2, not in those with a BRCa1 mutation.